WO2006039212A2 - Substituted 2h-1,3-benzoxazin-4(3h)-ones - Google Patents
Substituted 2h-1,3-benzoxazin-4(3h)-ones Download PDFInfo
- Publication number
- WO2006039212A2 WO2006039212A2 PCT/US2005/034246 US2005034246W WO2006039212A2 WO 2006039212 A2 WO2006039212 A2 WO 2006039212A2 US 2005034246 W US2005034246 W US 2005034246W WO 2006039212 A2 WO2006039212 A2 WO 2006039212A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alkyl
- group
- cycloalkyl
- alkoxy
- halogen
- Prior art date
Links
- 0 C*(C)Cc1cc(N(C(*)(*)Oc(c2c3)c(*)c(N(*)*)c3F)C2=O)ccc1C(NS(c1ccc[s]1)(=O)=O)=O Chemical compound C*(C)Cc1cc(N(C(*)(*)Oc(c2c3)c(*)c(N(*)*)c3F)C2=O)ccc1C(NS(c1ccc[s]1)(=O)=O)=O 0.000 description 2
- WUWKWUGTEGQQKZ-UHFFFAOYSA-N CC(Oc(c(C(O)=O)c1)cc(F)c1F)=O Chemical compound CC(Oc(c(C(O)=O)c1)cc(F)c1F)=O WUWKWUGTEGQQKZ-UHFFFAOYSA-N 0.000 description 1
- QCMZHPKXFCLHNU-UHFFFAOYSA-N CN(C)CCOc(cc(cc1)[N+]([O-])=O)c1NC(c(c(O)c1)cc(F)c1F)=O Chemical compound CN(C)CCOc(cc(cc1)[N+]([O-])=O)c1NC(c(c(O)c1)cc(F)c1F)=O QCMZHPKXFCLHNU-UHFFFAOYSA-N 0.000 description 1
- SKEJIURICADWEW-UHFFFAOYSA-N CNc(cc(c1c2)OCN(c(cc3)cc(C(N(C)C)=O)c3N)C1=O)c2F Chemical compound CNc(cc(c1c2)OCN(c(cc3)cc(C(N(C)C)=O)c3N)C1=O)c2F SKEJIURICADWEW-UHFFFAOYSA-N 0.000 description 1
- QJOYSGZVQSTCPT-UHFFFAOYSA-N COc(cc(cc1)[N+]([O-])=O)c1NC(c(c(O)c1)cc(F)c1F)=O Chemical compound COc(cc(cc1)[N+]([O-])=O)c1NC(c(c(O)c1)cc(F)c1F)=O QJOYSGZVQSTCPT-UHFFFAOYSA-N 0.000 description 1
- CTKPUPXVLFQXSI-UHFFFAOYSA-N Cc([s]1)ccc1S(NC(Nc(nc1)ccc1N(COc(c1c2)cc(NC)c2F)C1=O)=O)(=O)=O Chemical compound Cc([s]1)ccc1S(NC(Nc(nc1)ccc1N(COc(c1c2)cc(NC)c2F)C1=O)=O)(=O)=O CTKPUPXVLFQXSI-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P41/00—Drugs used in surgical methods, e.g. surgery adjuvants for preventing adhesion or for vitreum substitution
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Definitions
- ADP adenosine 5'- diphosphate
- ATP adenosine 5 '-triphosphate
- aryl means, unless otherwise stated, a polyunsaturated, typically aromatic, hydrocarbon group which can be a single ring or multiple rings (up to three rings) which are fused together or linked covalently.
- exemplary aryl groups are phenyl, naphthyl, biphenyl and the like.
- heteroaryl refers to aryl groups (or rings) that contain from one to five heteroatoms selected from N, O, and S, wherein the nitrogen and sulfur atoms are optionally oxidized, and the nitrogen atom(s) are optionally quaternized.
- a heteroaryl group can be attached to the remainder of the molecule through a heteroatom.
- salts of amino acids such as arginate and the like, and salts of organic acids like glucuronic or galactunoric acids and the like (see, for example, Berge, S.M., et al, "Pharmaceutical Salts", Journal of Pharmaceutical Science, 1977, 66, 1-19).
- Certain specific compounds of the present invention contain both basic and acidic functionalities that allow the compounds to be converted into either base or acid addition salts.
- R 1 is C 1-4 alkyl, C 3-5 cycloalkyl, C 3-5 cycloalkyl-alkyl, or halosubstituted benzyl
- R 2 is H
- R 3 is H, C 1-4 alkyl, C 2-4 alkenyl, C 2-4 alkynyl, C 3- 5 cycloalkyl, C 3-5 cycloalkyl-alkyl, C 1-4 haloalkyl, cyano or -C(O)R 3a
- R 4 is H or C 1-4 alkyl
- R 5 is H or C 1-4 alkyl, C 1-4 haloalkyl, -CN, -C ⁇ CH or -COlS]H 2
- R 6 when present is selected from the group consisting of halogen, C 1-4 alkyl, C 1-4 alkoxy, C 3-5 cycloalkyl-alkoxy, -O(CH
- the compounds of the invention are represented by the formula: wherein the subscript n is an integer of from 0 to 2.
- the remaining R groups (R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 ) have the meanings provided above with reference to general formula I.
- unlabeled bonds e.g., those with an unlabeled terminus
- methyl (CH 3 ) groups are meant to illustrate methyl (CH 3 ) groups.
- dissolution or suspension of the active compound in a vehicle such as an oil or a synthetic fatty vehicle like ethyl oleate, or into a liposome may be desired.
- a vehicle such as an oil or a synthetic fatty vehicle like ethyl oleate
- Buffers, preservatives, antioxidants and the like can be incorporated according to accepted pharmaceutical practice.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Obesity (AREA)
- Urology & Nephrology (AREA)
- Surgery (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007534673A JP2008514703A (ja) | 2004-09-29 | 2005-09-26 | 置換2h−1,3−ベンゾオキサジン−4(3h)−オン |
NZ554211A NZ554211A (en) | 2004-09-29 | 2005-09-26 | Substituted 2H-1,3-Benzoxazin-4(3H)-ones |
AU2005292314A AU2005292314B2 (en) | 2004-09-29 | 2005-09-26 | Substituted 2H-1,3-benzoxazin-4(3H)-ones |
MX2007003836A MX2007003836A (es) | 2004-09-29 | 2005-09-26 | 2h-1,3-benzoxazin-4(3h)-onas sustituidas. |
BRPI0516181-9A BRPI0516181A (pt) | 2004-09-29 | 2005-09-26 | composto e sais farmaceuticamente aceitáveis do mesmo, composição farmacêutica, e, métodos para tratar trombose em um indivìduo e para prevenir a ocorrência de um evento isquêmico secundário |
CN2005800328848A CN101031565B (zh) | 2004-09-29 | 2005-09-26 | 取代的2h-1,3-苯并噁嗪-4(3h)-酮 |
CA002581638A CA2581638A1 (en) | 2004-09-29 | 2005-09-26 | Substituted 2h-1,3-benzoxazin-4(3h)-ones |
EP05798632A EP1812429A4 (en) | 2004-09-29 | 2005-09-26 | SUBSTITUTED 2H-1,3-BENZOXAZIN-4 (3H) -ONE |
IL182180A IL182180A0 (en) | 2004-09-29 | 2007-03-26 | 2h-1,3-benzoxazin-4(3h)-one derivatives and pharmaceutical compositions containing the same |
HK08102004.2A HK1111414A1 (en) | 2004-09-29 | 2008-02-22 | Substituted 2h-1,3-benzoxazin-4(3h)-ones |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US61456404P | 2004-09-29 | 2004-09-29 | |
US60/614,564 | 2004-09-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2006039212A2 true WO2006039212A2 (en) | 2006-04-13 |
WO2006039212A3 WO2006039212A3 (en) | 2007-01-25 |
Family
ID=36142983
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2005/034246 WO2006039212A2 (en) | 2004-09-29 | 2005-09-26 | Substituted 2h-1,3-benzoxazin-4(3h)-ones |
Country Status (14)
Country | Link |
---|---|
US (1) | US7205296B2 (zh) |
EP (1) | EP1812429A4 (zh) |
JP (1) | JP2008514703A (zh) |
KR (1) | KR20070064356A (zh) |
CN (1) | CN101031565B (zh) |
AU (1) | AU2005292314B2 (zh) |
BR (1) | BRPI0516181A (zh) |
CA (1) | CA2581638A1 (zh) |
HK (1) | HK1111414A1 (zh) |
IL (1) | IL182180A0 (zh) |
MX (1) | MX2007003836A (zh) |
NZ (1) | NZ554211A (zh) |
WO (1) | WO2006039212A2 (zh) |
ZA (1) | ZA200702688B (zh) |
Cited By (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008036843A3 (en) * | 2006-09-20 | 2008-05-15 | Portola Pharm Inc | Nitrogen containing substituted heterocycles as platelet adp receptor inhibitors |
US9481677B2 (en) | 2011-10-31 | 2016-11-01 | Xenon Pharmaceuticals Inc. | Biaryl ether sulfonamides and their use as therapeutic agents |
US9493429B2 (en) | 2013-03-15 | 2016-11-15 | Genentech, Inc. | Substituted benzoxazoles and methods of use thereof |
US9546164B2 (en) | 2013-11-27 | 2017-01-17 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
US9550775B2 (en) | 2013-03-14 | 2017-01-24 | Genentech, Inc. | Substituted triazolopyridines and methods of use thereof |
US9630929B2 (en) | 2011-10-31 | 2017-04-25 | Xenon Pharmaceuticals Inc. | Benzenesulfonamide compounds and their use as therapeutic agents |
US9771376B2 (en) | 2000-05-22 | 2017-09-26 | Genentech, Inc. | N-substituted benzamides and methods of use thereof |
US9782408B2 (en) | 2014-10-06 | 2017-10-10 | Vertex Pharmaceuticals Incorporated | Modulators of cystic fibrosis transmembrane conductance regulator |
US10005724B2 (en) | 2014-07-07 | 2018-06-26 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
US10071957B2 (en) | 2012-07-06 | 2018-09-11 | Genentech, Inc. | N-substituted benzamides and methods of use thereof |
US10179767B2 (en) | 2015-05-22 | 2019-01-15 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
US10457654B2 (en) | 2016-10-17 | 2019-10-29 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
US10538487B2 (en) | 2015-02-16 | 2020-01-21 | The University Of Queensland | Sulfonylureas and related compounds and use of same |
US10570115B2 (en) | 2016-09-30 | 2020-02-25 | Vertex Pharmaceuticals Incorporated | Modulator of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator |
US10654829B2 (en) | 2017-10-19 | 2020-05-19 | Vertex Pharmaceuticals Incorporated | Crystalline forms and compositions of CFTR modulators |
US10738030B2 (en) | 2016-03-31 | 2020-08-11 | Vertex Pharmaceuticals Incorporated | Modulators of cystic fibrosis transmembrane conductance regulator |
US10766858B2 (en) | 2016-03-30 | 2020-09-08 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
US10787446B2 (en) | 2015-09-28 | 2020-09-29 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
US10793547B2 (en) | 2016-12-09 | 2020-10-06 | Vertex Pharmaceuticals Incorporated | Modulator of the cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator |
US10899732B2 (en) | 2015-11-25 | 2021-01-26 | Genentech, Inc. | Substituted benzamides useful as sodium channel blockers |
US10947251B2 (en) | 2018-03-30 | 2021-03-16 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
US11028075B2 (en) | 2018-02-26 | 2021-06-08 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
US11130726B2 (en) | 2015-08-27 | 2021-09-28 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
US11179367B2 (en) | 2018-02-05 | 2021-11-23 | Vertex Pharmaceuticals Incorporated | Pharmaceutical compositions for treating cystic fibrosis |
US11253509B2 (en) | 2017-06-08 | 2022-02-22 | Vertex Pharmaceuticals Incorporated | Methods of treatment for cystic fibrosis |
US11414439B2 (en) | 2018-04-13 | 2022-08-16 | Vertex Pharmaceuticals Incorporated | Modulators of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator |
US11434201B2 (en) | 2017-08-02 | 2022-09-06 | Vertex Pharmaceuticals Incorporated | Processes for preparing pyrrolidine compounds |
US11465985B2 (en) | 2017-12-08 | 2022-10-11 | Vertex Pharmaceuticals Incorporated | Processes for making modulators of cystic fibrosis transmembrane conductance regulator |
US11465992B2 (en) | 2017-07-07 | 2022-10-11 | Inflazome Limited | Sulfonamide carboxamide compounds |
US11517564B2 (en) | 2017-07-17 | 2022-12-06 | Vertex Pharmaceuticals Incorporated | Methods of treatment for cystic fibrosis |
US11542255B2 (en) | 2017-08-15 | 2023-01-03 | Inflazome Limited | Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors |
US11613542B2 (en) | 2017-08-15 | 2023-03-28 | Inflazome Limited | Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors |
EP4074707A4 (en) * | 2019-12-10 | 2024-01-03 | Shanghai Zhimeng Biopharma, Inc. | COMPOUND WITH NEUROPROTECTIVE EFFECT, PREPARATION METHOD AND USE THEREOF |
US11905252B2 (en) | 2018-03-02 | 2024-02-20 | Inflazome Limited | Compounds |
US11926600B2 (en) | 2017-08-15 | 2024-03-12 | Inflazome Limited | Sulfonylureas and sulfonylthioureas as NLRP3 inhibitors |
US12012392B2 (en) | 2017-11-09 | 2024-06-18 | Inflazome Limited | Sulfonamide carboxamide compounds |
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US7740693B2 (en) * | 2007-10-01 | 2010-06-22 | Honeywell International Inc. | Organic fluorescent sulfonyl ureido benzoxazinone pigments |
US9469654B2 (en) | 2012-09-27 | 2016-10-18 | Portola Pharmaceuticals, Inc. | Bicyclic oxa-lactam kinase inhibitors |
PL3177612T3 (pl) | 2014-08-04 | 2022-08-08 | Nuevolution A/S | Opcjonalnie skondensowane pochodne pirymidyny podstawione heterocyklilem, użyteczne w leczeniu chorób zapalnych, metabolicznych, onkologicznych i autoimmunologicznych |
JP2020511511A (ja) | 2017-03-24 | 2020-04-16 | ジェネンテック, インコーポレイテッド | ナトリウムチャネル阻害剤としての4−ピペリジン−n−(ピリミジン−4−イル)クロマン−7−スルホンアミド誘導体 |
WO2019074979A1 (en) | 2017-10-09 | 2019-04-18 | Girafpharma, Llc | HETEROCYCLIC COMPOUNDS AND USES THEREOF |
EP3694509A4 (en) | 2017-10-09 | 2021-07-14 | Nuvation Bio Inc. | HETEROCYCLIC COMPOUNDS AND THEIR USES |
WO2020210377A1 (en) * | 2019-04-09 | 2020-10-15 | Nuvation Bio Inc. | Heterocyclic compounds and uses thereof |
WO2020210383A1 (en) * | 2019-04-09 | 2020-10-15 | Nuvation Bio Inc. | Heterocyclic compounds and uses thereof |
JP2022526831A (ja) | 2019-04-09 | 2022-05-26 | ニューベイション・バイオ・インコーポレイテッド | ヘテロ環式化合物およびその使用 |
MX2022007265A (es) | 2019-12-20 | 2022-09-09 | Nuevolution As | Compuestos activos frente a receptores nucleares. |
WO2021198955A1 (en) | 2020-03-31 | 2021-10-07 | Nuevolution A/S | Compounds active towards nuclear receptors |
WO2021198956A1 (en) | 2020-03-31 | 2021-10-07 | Nuevolution A/S | Compounds active towards nuclear receptors |
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FI101150B (fi) | 1991-09-09 | 1998-04-30 | Sankyo Co | Menetelmä lääkeaineina käyttökelpoisten tetrahydrotienopyridiinin johd annaisten valmistamiseksi |
FR2702477B1 (fr) * | 1993-03-08 | 1995-04-28 | Synthelabo | Dérivés de benzoxazine, leur préparation et leur application en thérapeutique. |
JP3814742B2 (ja) * | 1996-10-18 | 2006-08-30 | イハラケミカル工業株式会社 | 4−フルオロサリチル酸類 |
SE9702774D0 (sv) | 1997-07-22 | 1997-07-22 | Astra Pharma Prod | Novel compounds |
WO1999036425A1 (en) | 1998-01-15 | 1999-07-22 | Cor Therapeutics, Inc. | Platelet adp receptor inhibitors |
JP4588877B2 (ja) | 1998-06-17 | 2010-12-01 | ブリストル−マイヤーズ スクイブ カンパニー | Adp−受容体抗血小板物質と抗高血圧薬の組合せ投与による脳梗塞の予防 |
US6509348B1 (en) | 1998-11-03 | 2003-01-21 | Bristol-Myers Squibb Company | Combination of an ADP-receptor blocking antiplatelet drug and a thromboxane A2 receptor antagonist and a method for inhibiting thrombus formation employing such combination |
JP4574100B2 (ja) * | 2000-02-04 | 2010-11-04 | ポートラ ファーマシューティカルズ, インコーポレイテッド | 血小板adpレセプターインヒビター |
US6906063B2 (en) * | 2000-02-04 | 2005-06-14 | Portola Pharmaceuticals, Inc. | Platelet ADP receptor inhibitors |
ATE357457T1 (de) | 2000-11-01 | 2007-04-15 | Astellas Pharma Inc | Verfahren zum screenen eines plättchenhemmers |
US6861424B2 (en) | 2001-06-06 | 2005-03-01 | Schering Aktiengesellschaft | Platelet adenosine diphosphate receptor antagonists |
CN1735603A (zh) * | 2002-12-06 | 2006-02-15 | 东丽株式会社 | 苯并吗啉衍生物 |
MXPA06003625A (es) * | 2003-10-03 | 2006-08-11 | Portola Pharm Inc | Isoquinolinonas sustituidas. |
DE602004024093D1 (de) * | 2003-10-03 | 2009-12-24 | Portola Pharm Inc | 2,4-dioxo-3-chinazolinylarylsulfonylharnstoffe |
-
2005
- 2005-09-26 KR KR1020077009902A patent/KR20070064356A/ko not_active Application Discontinuation
- 2005-09-26 US US11/236,051 patent/US7205296B2/en active Active
- 2005-09-26 BR BRPI0516181-9A patent/BRPI0516181A/pt not_active IP Right Cessation
- 2005-09-26 ZA ZA200702688A patent/ZA200702688B/en unknown
- 2005-09-26 CN CN2005800328848A patent/CN101031565B/zh not_active Expired - Fee Related
- 2005-09-26 EP EP05798632A patent/EP1812429A4/en not_active Withdrawn
- 2005-09-26 NZ NZ554211A patent/NZ554211A/en not_active IP Right Cessation
- 2005-09-26 JP JP2007534673A patent/JP2008514703A/ja not_active Ceased
- 2005-09-26 CA CA002581638A patent/CA2581638A1/en not_active Abandoned
- 2005-09-26 MX MX2007003836A patent/MX2007003836A/es active IP Right Grant
- 2005-09-26 AU AU2005292314A patent/AU2005292314B2/en not_active Ceased
- 2005-09-26 WO PCT/US2005/034246 patent/WO2006039212A2/en active Application Filing
-
2007
- 2007-03-26 IL IL182180A patent/IL182180A0/en unknown
-
2008
- 2008-02-22 HK HK08102004.2A patent/HK1111414A1/xx not_active IP Right Cessation
Non-Patent Citations (1)
Title |
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See references of EP1812429A4 * |
Cited By (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9771376B2 (en) | 2000-05-22 | 2017-09-26 | Genentech, Inc. | N-substituted benzamides and methods of use thereof |
JP2010504357A (ja) * | 2006-09-20 | 2010-02-12 | ポートラ ファーマシューティカルズ, インコーポレイテッド | 血小板adp受容体阻害剤としての窒素含有置換ヘテロ環 |
US7834023B2 (en) | 2006-09-20 | 2010-11-16 | Portola Pharmaceuticals, Inc. | Substituted dihydroquinazolines as platelet ADP receptor inhibitors |
WO2008036843A3 (en) * | 2006-09-20 | 2008-05-15 | Portola Pharm Inc | Nitrogen containing substituted heterocycles as platelet adp receptor inhibitors |
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AU2005292314B2 (en) | 2011-11-03 |
CN101031565B (zh) | 2010-09-29 |
IL182180A0 (en) | 2007-07-24 |
WO2006039212A3 (en) | 2007-01-25 |
BRPI0516181A (pt) | 2008-08-26 |
HK1111414A1 (en) | 2008-08-08 |
CN101031565A (zh) | 2007-09-05 |
CA2581638A1 (en) | 2006-04-13 |
EP1812429A4 (en) | 2010-07-21 |
US20060069093A1 (en) | 2006-03-30 |
EP1812429A2 (en) | 2007-08-01 |
KR20070064356A (ko) | 2007-06-20 |
AU2005292314A1 (en) | 2006-04-13 |
JP2008514703A (ja) | 2008-05-08 |
NZ554211A (en) | 2010-10-29 |
ZA200702688B (en) | 2008-06-25 |
MX2007003836A (es) | 2007-08-20 |
US7205296B2 (en) | 2007-04-17 |
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